BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 18258490)

  • 1. Sharing genetic test results in Lynch syndrome: communication with close and distant relatives.
    Stoffel EM; Ford B; Mercado RC; Punglia D; Kohlmann W; Conrad P; Blanco A; Shannon KM; Powell M; Gruber SB; Terdiman J; Chung DC; Syngal S
    Clin Gastroenterol Hepatol; 2008 Mar; 6(3):333-8. PubMed ID: 18258490
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis.
    Petersen J; Koptiuch C; Wu YP; Mooney R; Elrick A; Szczotka K; Keener M; Pappas L; Kanth P; Soisson A; Kohlmann W; Kaphingst KA
    Patient Educ Couns; 2018 Nov; 101(11):2011-2017. PubMed ID: 30097381
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review.
    Sharaf RN; Myer P; Stave CD; Diamond LC; Ladabaum U
    Clin Gastroenterol Hepatol; 2013 Sep; 11(9):1093-100. PubMed ID: 23669308
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Improving the uptake of predictive testing and colorectal screening in Lynch syndrome: a regional primary care survey.
    Barrow P; Green K; Clancy T; Lalloo F; Hill J; Evans DG
    Clin Genet; 2015 Jun; 87(6):517-24. PubMed ID: 25652327
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.
    Dilzell K; Kingham K; Ormond K; Ladabaum U
    Fam Cancer; 2014 Sep; 13(3):381-9. PubMed ID: 24770865
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome.
    Aktan-Collan KI; Kääriäinen HA; Kolttola EM; Pylvänäinen K; Järvinen HJ; Haukkala AH; Mecklin JP
    Fam Cancer; 2011 Mar; 10(1):43-50. PubMed ID: 20857224
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Extent of Pedigree Required to Screen for and Diagnose Hereditary Nonpolyposis Colorectal Cancer: Comparison of Simplified and Extended Pedigrees.
    Heo Y; Kim MH; Kim DW; Lee SA; Bang S; Kim MJ; Oh HK; Kang SB; Kang SI; Park JW; Ryoo SB; Jeong SY; Park KJ
    Dis Colon Rectum; 2020 Feb; 63(2):152-159. PubMed ID: 31842160
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic testing in families with hereditary colorectal cancer in British Columbia and Yukon: a retrospective cross-sectional analysis.
    Beard VK; Bedard AC; Nuk J; Lee PWC; Hong Q; Bedard JEJ; Sun S; Schrader KA
    CMAJ Open; 2020; 8(4):E637-E642. PubMed ID: 33077534
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Stakeholder Perspectives on Overcoming Barriers to Cascade Testing in Lynch Syndrome: A Qualitative Study.
    Srinivasan S; Hampel H; Leeman J; Patel A; Kulchak Rahm A; Reuland DS; Roberts MC
    Cancer Prev Res (Phila); 2020 Dec; 13(12):1037-1046. PubMed ID: 32727822
    [TBL] [Abstract][Full Text] [Related]  

  • 10. How families communicate about HNPCC genetic testing: findings from a qualitative study.
    Peterson SK; Watts BG; Koehly LM; Vernon SW; Baile WF; Kohlmann WK; Gritz ER
    Am J Med Genet C Semin Med Genet; 2003 May; 119C(1):78-86. PubMed ID: 12704641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
    Yurgelun MB; Allen B; Kaldate RR; Bowles KR; Judkins T; Kaushik P; Roa BB; Wenstrup RJ; Hartman AR; Syngal S
    Gastroenterology; 2015 Sep; 149(3):604-13.e20. PubMed ID: 25980754
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families.
    Burton-Chase AM; Hovick SR; Peterson SK; Marani SK; Vernon SW; Amos CI; Frazier ML; Lynch PM; Gritz ER
    Clin Genet; 2013 Mar; 83(3):215-20. PubMed ID: 23414081
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic testing for Lynch syndrome: family communication and motivation.
    Leenen CH; Heijer Md; van der Meer C; Kuipers EJ; van Leerdam ME; Wagner A
    Fam Cancer; 2016 Jan; 15(1):63-73. PubMed ID: 26446592
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.
    Bonis PA; Trikalinos TA; Chung M; Chew P; Ip S; DeVine DA; Lau J
    Evid Rep Technol Assess (Full Rep); 2007 May; (150):1-180. PubMed ID: 17764220
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.
    Menko FH; Ter Stege JA; van der Kolk LE; Jeanson KN; Schats W; Moha DA; Bleiker EMA
    Fam Cancer; 2019 Jan; 18(1):127-135. PubMed ID: 29846880
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members.
    Järvinen HJ; Renkonen-Sinisalo L; Aktán-Collán K; Peltomäki P; Aaltonen LA; Mecklin JP
    J Clin Oncol; 2009 Oct; 27(28):4793-7. PubMed ID: 19720893
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives.
    Hunter JE; Arnold KA; Cook JE; Zepp J; Gilmore MJ; Rope AF; Davis JV; Bergen KM; Esterberg E; Muessig KR; Peterson SK; Syngal S; Acheson L; Wiesner G; Reiss J; Goddard KAB
    Fam Cancer; 2017 Jul; 16(3):377-387. PubMed ID: 28176204
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Communication of genetic test results to family and health-care providers following disclosure of research results.
    Graves KD; Sinicrope PS; Esplen MJ; Peterson SK; Patten CA; Lowery J; Sinicrope FA; Nigon SK; Borgen J; Gorin SS; Keogh LA; Lindor NM;
    Genet Med; 2014 Apr; 16(4):294-301. PubMed ID: 24091800
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment.
    Ishii N; Arai M; Koyama Y; Ueno M; Yamaguchi T; Kazuma K; Muto T
    Fam Cancer; 2011 Dec; 10(4):649-54. PubMed ID: 21695501
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Family communication about positive BRCA1 and BRCA2 genetic test results.
    McGivern B; Everett J; Yager GG; Baumiller RC; Hafertepen A; Saal HM
    Genet Med; 2004; 6(6):503-9. PubMed ID: 15545746
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.